JP2006206565A - Pranoprofen-containing composition - Google Patents
Pranoprofen-containing composition Download PDFInfo
- Publication number
- JP2006206565A JP2006206565A JP2005056421A JP2005056421A JP2006206565A JP 2006206565 A JP2006206565 A JP 2006206565A JP 2005056421 A JP2005056421 A JP 2005056421A JP 2005056421 A JP2005056421 A JP 2005056421A JP 2006206565 A JP2006206565 A JP 2006206565A
- Authority
- JP
- Japan
- Prior art keywords
- composition
- sodium
- acid
- hydrochloride
- eye
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 99
- TVQZAMVBTVNYLA-UHFFFAOYSA-N Pranoprofen Chemical compound C1=CC=C2CC3=CC(C(C(O)=O)C)=CC=C3OC2=N1 TVQZAMVBTVNYLA-UHFFFAOYSA-N 0.000 title claims abstract description 29
- 229960003101 pranoprofen Drugs 0.000 title claims abstract description 28
- 150000003839 salts Chemical class 0.000 claims abstract description 41
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- 238000002835 absorbance Methods 0.000 claims description 10
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- 235000019162 flavin adenine dinucleotide Nutrition 0.000 claims description 6
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- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 12
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Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Description
本発明は、プラノプロフェンまたはその塩、およびビタミンB2類による疲れ目の改善に関する。 The present invention, pranoprofen or a salt thereof, and to the improvement of eyestrain due to vitamin B 2 compounds.
近年、目の疲れを訴える人が増加するに伴ってその解決方法が望まれており、例えば点眼薬や内服薬、温感や冷感を与える商品、目周辺のマッサージ機など多岐にわたって目の疲れを取る商品が開発されている。
目の疲れの原因として、読書、注視作業、観察作業などの目の酷使や精神的緊張によるものが挙げられるが、パーソナルコンピューターの普及に伴い急激に増加してきたVDT(Visual Display Terminal)作業による目の疲れが非常に多くなっている。特にコンタクトレンズ装用者ではVDT作業による目の疲れを訴えるものが多い。そして、目の疲れを訴える患者は、目の奥の痛み、眼のかすみ、目の乾き、肩こり、頭重などの症状を伴うことが一般的であり、目の疲れが甚だしい時には、悪心、吐気をも伴う場合がある。これらの症状は毛様体筋が長時間の注視作業などにより過度の緊張状態に陥り、目の調節機能が低下することが要因となって起こることが指摘されている。
In recent years, as the number of people who complain of eye fatigue has increased, a solution has been desired. For example, eye drops and internal medicines, products that give warmth and coolness, massage machines around the eyes, etc. Products to be taken have been developed.
Causes of eye fatigue include reading, gazing, and observation due to overuse of the eye and mental tension. Eyes due to VDT (Visual Display Terminal) work, which has increased rapidly with the spread of personal computers. The tiredness of has become very much. In particular, many contact lens wearers complain of eye fatigue due to VDT work. Patients who complain of eye fatigue usually have symptoms such as pain in the back of the eye, blurred vision, dry eyes, stiff shoulders, and head weight. When the eyestrain is severe, nausea and nausea May also accompany. It has been pointed out that these symptoms are caused by the ciliary muscles becoming excessively tense due to long-term gaze work and the like, and the regulation function of the eyes is lowered.
目の疲れを改善する点眼剤としては、ビタミンB2類をはじめとするビタミン類やアミノ酸類などを含有したものなどが数多く知られている。中でも補酵素型ビタミンB2類であるフラビンアデニンジヌクレオチドは、目の疲労を回復し、眼組織、特に角膜の新陳代謝を活性化することが知られている(特許文献1:特開平08-104636号公報)。さらに、フラビンアデニンジヌクレオチドは、抗アレルギ−・抗炎症作用(特許文献2:特開昭63-188627号公報)、ブドウ膜炎治療作用(特許文献3:特開平08-225451号公報)、目の乾きの改善(特許文献4:特開平11-263729号公報)なども知られている。
一方、プラノプロフェンは優れた抗炎症作用、鎮痛作用、解熱作用を持つ、安全性の高いプロピオン酸系の酸性非ステロイド系抗炎症剤として知られており、点眼剤や錠剤、カプセル剤、シロップ剤等の内服剤などの形態で広く使用されているが、目の疲れに対する効果はこれまで知られていない。さらに、プラノプロフェンは光に晒されると経時的に分解するため遮光保存する必要がある。特に、水の存在下では著しく不安定になる上不溶物が生じやすく、点眼剤などの水性組成物は長期間保存すると溶液の澄明性が損なわれ、外観が悪化してしまうという問題点もある。
Many eye drops for improving eye fatigue include vitamin B 2 and other vitamins and amino acids. Flavin adenine dinucleotide is inter alia coenzyme vitamin B 2 such, recovered eye fatigue, ocular tissue, especially those known to activate the metabolism of the cornea (Patent Document 1: JP-A-08-104636 Issue gazette). Furthermore, flavin adenine dinucleotide has an anti-allergic and anti-inflammatory action (Patent Document 2: JP-A-63-188627), an uveitis therapeutic action (Patent Document 3: JP-A-08-225451), Also known is improvement of dryness (Patent Document 4: Japanese Patent Laid-Open No. 11-263729).
On the other hand, pranoprofen is known as a highly safe acidic non-steroidal anti-inflammatory agent of propionic acid type with excellent anti-inflammatory, analgesic and antipyretic effects, and is an eye drop, tablet, capsule, syrup Although it is widely used in the form of an internal medicine such as an agent, the effect on eye fatigue has not been known so far. Furthermore, since pranoprofen decomposes with time when exposed to light, it needs to be stored in the dark. In particular, in the presence of water, it becomes extremely unstable and insoluble matter is likely to be produced. When stored for a long period of time, aqueous compositions such as eye drops impair the clarity of the solution and deteriorate the appearance. .
本発明の目的は、目の疲れに対する改善効果が高い組成物を提供することにある。 An object of the present invention is to provide a composition having a high effect of improving eye fatigue.
本発明者等は、上記課題を解決すべく鋭意検討したところ、プラノプロフェン又はその塩を含有する組成物にビタミンB2類を配合することで、目の疲れに対する改善効果が顕著となることを見出し、本発明を完成した。 The present inventors diligently studied to solve the above problems, and the effect of improving eye fatigue becomes remarkable by adding vitamin B 2 to a composition containing pranoprofen or a salt thereof. The present invention has been completed.
すなわち、本発明は下記(1)〜(15)に掲げる組成物である。
(1)プラノプロフェン又はその塩、およびビタミンB2類を含有する組成物。
(2)ビタミンB2類が、フラビンアデニンジヌクレオチドまたはその塩である(1)に記載の組成物。
(3)さらに、モノテルペノイドを含有する(1)または(2)に記載の組成物。
(4)さらに、粘稠剤、非イオン性界面活性剤、キレート剤、防腐剤、緩衝剤およびpH調整剤からなる群から選択される1種又は2種以上を含有する(1)〜(3)に記載の組成物。
(5)プラノプロフェンを含有する、目の疲れ改善用組成物。
(6)組成物が、点眼剤、点鼻剤、洗眼剤、コンタクトレンズ用剤、内服剤である(1)〜(5)のいずれかに記載の組成物。
(7)組成物が、水性組成物である(1)〜(6)のいずれかに記載の組成物。
(8)組成物が、眼科用組成物である(1)〜(5)のいずれかに記載の組成物。
(9)組成物が、目の疲れ改善用点眼剤又は洗眼剤である(1)〜(4)のいずれかに記載の組成物。
(10)340nm〜380nmの平均吸光度が1.0以上である容器に収容されてなることを特徴とする(1)〜(9)のいずれかに記載の組成物。
(11)容器が、ポリエチレンナフタレート、ポリアリレート、ポリエチレンテレフタレート、ポリプロピレン、ポリエチレンのいずれか1種、これらの共重合ポリエステル、または2種以上の混合体を主原料として構成された容器である(10)に記載の組成物。
(12)容器が、ポリエチレンナフタレート、ポリアリレート、またはこれらの共重合ポリエステルを主原料として構成された容器である(10)記載の組成物。
(13)容器が、ポリエチレンナフタレート、ポリアリレートまたはこれらの共重合ポリエステルのいずれか1種以上と、ポリエチレンテレフタレート、ポリプロピレン、ポリエチレンのいずれか1種以上の混合体を主原料として構成された容器である(10)記載の組成物。
(14)容器が、ポリエチレンナフタレート、ポリアリレート、これらの共重合ポリエステル、ポリエチレンテレフタレート、ポリプロピレン、ポリエチレンから選択される1種、または2種以上の混合体を主原料として、紫外線遮断剤を添加またはコーティングした素材で構成された容器である(10)記載の水性組成物。
(15)容器が、紫外線遮断剤を添加またはコーティングされた容器である(10)〜(14)のいずれかに記載の組成物。
That is, this invention is a composition hung up to the following (1)-(15).
(1) A composition containing pranoprofen or a salt thereof, and vitamin B 2 .
(2) The composition according to (1), wherein the vitamin B 2 is flavin adenine dinucleotide or a salt thereof.
(3) The composition according to (1) or (2), further comprising a monoterpenoid.
(4) Furthermore, 1 type or 2 types or more selected from the group which consists of a thickener, a nonionic surfactant, a chelating agent, a preservative, a buffering agent, and a pH adjuster are contained (1)-(3 ).
(5) A composition for improving eye fatigue, comprising pranoprofen.
(6) The composition according to any one of (1) to (5), wherein the composition is an eye drop, a nose drop, an eye wash, a contact lens preparation, or an internal preparation.
(7) The composition according to any one of (1) to (6), wherein the composition is an aqueous composition.
(8) The composition according to any one of (1) to (5), wherein the composition is an ophthalmic composition.
(9) The composition according to any one of (1) to (4), wherein the composition is an eye drop or eye wash for improving eye fatigue.
(10) The composition according to any one of (1) to (9), which is contained in a container having an average absorbance of 340 nm to 380 nm of 1.0 or more.
(11) The container is a container composed mainly of any one of polyethylene naphthalate, polyarylate, polyethylene terephthalate, polypropylene, polyethylene, a copolymer polyester thereof, or a mixture of two or more kinds (10 ).
(12) The composition according to (10), wherein the container is a container composed mainly of polyethylene naphthalate, polyarylate, or a copolymer polyester thereof.
(13) A container in which a main raw material is a mixture of at least one of polyethylene naphthalate, polyarylate, or a copolymer polyester thereof, and at least one of polyethylene terephthalate, polypropylene, and polyethylene. The composition according to (10).
(14) The container is composed of one or more selected from polyethylene naphthalate, polyarylate, copolymerized polyesters thereof, polyethylene terephthalate, polypropylene, and polyethylene, and a UV blocking agent is added as a main raw material. The aqueous composition according to (10), which is a container composed of a coated material.
(15) The composition according to any one of (10) to (14), wherein the container is a container to which an ultraviolet blocking agent is added or coated.
本発明は、プラノプロフェン又はその塩、およびビタミンB2類を含有することで、目の疲れを顕著に改善することができる。 The present invention can remarkably improve eye fatigue by containing pranoprofen or a salt thereof and vitamin B 2 .
本明細書中、特に言及しない限り、%はw/v%を意味するものとする。また、コンタクトレンズという語句は、特記しない限り、ハード、酸素透過性ハード、ソフト等のあらゆるタイプのコンタクトレンズを包含する意味で用いる。
また、本明細書中、「塩」とは薬理学的に又は生理学的に許容される塩を意味する。
さらに、本明細書中、水性組成物とは、組成物中に水を少なくとも5重量%以上、好ましくは20重量%以上、更に好ましくは50重量%以上含有するものを意味する。
In the present specification, unless otherwise specified,% means w / v%. Further, the term “contact lens” is used in the meaning of including all types of contact lenses such as hard, oxygen-permeable hard, and soft unless otherwise specified.
In the present specification, “salt” means a pharmacologically or physiologically acceptable salt.
Furthermore, in the present specification, the aqueous composition means a composition containing at least 5% by weight, preferably 20% by weight or more, more preferably 50% by weight or more of water in the composition.
本発明の組成物に含有されるプラノプロフェン、即ちα−メチル−5H−[1]ベンゾピラノ[2,3−b]ピリジン−7−酢酸は公知化合物であり、公知の方法により合成してもよく市販品として入手することもできる。 Planoprofen, that is, α-methyl-5H- [1] benzopyrano [2,3-b] pyridine-7-acetic acid contained in the composition of the present invention is a known compound and can be synthesized by a known method. It can also be obtained as a commercial product.
また、プラノプロフェンの塩は、医薬上、薬理学的に又は生理学的に許容されることを限度として、特に制限されるものではない。このような塩としては、例えば、無機塩基との塩[例えば、ナトリウム塩、カリウム塩、カルシウム塩、マグネシウム塩、アルミニウム塩等]や、有機塩基との塩[例えば、メチルアミン、トリエチルアミン、ジエチルアミン、トリエタノールアミン、モルホリン、ピペラジン、ピロリジン、トリピリジン、ピコリン等の有機塩基との塩]などが挙げられる。
また、プラノプロフェン又はその塩は、水和物の形態でも使用できる。
The salt of pranoprofen is not particularly limited as long as it is pharmaceutically, pharmacologically or physiologically acceptable. Examples of such salts include salts with inorganic bases [eg, sodium salts, potassium salts, calcium salts, magnesium salts, aluminum salts, etc.] and salts with organic bases [eg, methylamine, triethylamine, diethylamine, And salts with organic bases such as triethanolamine, morpholine, piperazine, pyrrolidine, tripyridine, picoline] and the like.
Planoprofen or a salt thereof can also be used in the form of a hydrate.
これらのプラノプロフェン及びその塩は、1種単独で又は二種以上組み合わせて使用できる。好ましくはプラノプロフェンである。 These pranoprofen and its salt can be used individually by 1 type or in combination of 2 or more types. Pranoprofen is preferred.
本発明の組成物において、配合するプラノプロフェン又はその塩の割合は、本発明の効果が得られれば特に制限はないが、例えば、水性組成物の場合、0.0001〜2w/v%、好ましくは0.0005〜0.2w/v%、特に好ましくは0.001〜0.1w/v%程度である。具体的には、点眼剤の場合は、0.01〜0.1w/v%、好ましくは0.01〜0.05w/v%程度、点鼻剤、洗眼剤またはコンタクトレンズ用剤の場合は、0.001〜0.01w/v%、好ましくは0.001〜0.005w/v%、シロップ剤の場合は、0.1〜2w/v%、好ましくは0.5〜1.5w/v%である。
また、固形組成物の場合、8〜90重量%、好ましくは12〜80重量%である。具体的には、錠剤の場合は、1錠(100〜250mg)あたり20〜100mg、好ましくは30〜80mg程度で前記の重量%に含まれる範囲であればよい。成人一日服用量では、例えば0.1〜10000mg、好ましくは1〜1000mg程度に含まれる範囲であればよい。
In the composition of the present invention, the proportion of pranoprofen or a salt thereof to be blended is not particularly limited as long as the effects of the present invention are obtained. For example, in the case of an aqueous composition, 0.0001 to 2 w / v%, preferably It is about 0.0005 to 0.2 w / v%, particularly preferably about 0.001 to 0.1 w / v%. Specifically, in the case of eye drops, 0.01 to 0.1 w / v%, preferably about 0.01 to 0.05 w / v%, and in the case of nasal drops, eyewashes or contact lens preparations, 0.001 to 0.01 w / v. v%, preferably 0.001 to 0.005 w / v%, and in the case of syrup, 0.1 to 2 w / v%, preferably 0.5 to 1.5 w / v%.
Moreover, in the case of a solid composition, it is 8 to 90 weight%, Preferably it is 12 to 80 weight%. Specifically, in the case of a tablet, it may be in the range of 20 to 100 mg, preferably about 30 to 80 mg per tablet (100 to 250 mg) and included in the above-mentioned weight%. The daily dose for an adult may be within a range of, for example, about 0.1 to 10,000 mg, preferably about 1 to 1000 mg.
本発明の組成物に含有されるビタミンB2類は、公知化合物であり、公知の方法により合成してもよく市販品として入手することもできる。
ビタミンB2類としては、例えば、リボフラビン、リン酸リボフラビン、酪酸リボフラビン、酢酸リボフラビン、フラビンアデニンジヌクレオチド、フラビンモノヌクレオチドなどが挙げられる。また、ビタミンB2類は、ナトリウム塩、カリウム塩などの無機塩基との塩であっても良く、例えば、リン酸リボフラビンナトリウム、フラビンアデニンジヌクレオチドナトリウムなどが挙げられる。これらのビタミンB2類の中で、好ましくはリン酸リボフラビン、リン酸リボフラビンナトリウム、酪酸リボフラビン、フラビンアデニンジヌクレオチド、フラビンアデニンジヌクレオチドナトリウムであり、特に好ましくはフラビンアデニンジヌクレオチドナトリウムである。
The vitamin B 2 contained in the composition of the present invention is a known compound, and may be synthesized by a known method or obtained as a commercial product.
Examples of vitamin B 2 include riboflavin, riboflavin phosphate, riboflavin butyrate, riboflavin acetate, flavin adenine dinucleotide, and flavin mononucleotide. Vitamin B 2 may be a salt with an inorganic base such as sodium salt or potassium salt, and examples thereof include sodium riboflavin phosphate and sodium flavin adenine dinucleotide. Among these vitamin B 2 , riboflavin phosphate, sodium riboflavin phosphate, riboflavin butyrate, flavin adenine dinucleotide, and flavin adenine dinucleotide sodium are preferable, and flavin adenine dinucleotide sodium is particularly preferable.
本発明の組成物において、配合するビタミンB2類の割合は、本発明の効果が得られれば特に制限はないが、例えば、水性組成物の場合、0.0005〜0.1w/v%、好ましくは0.001〜0.05w/v%程度である。具体的には、点眼剤の場合は、0.005〜0.1w/v%、好ましくは0.01〜0.05w/v%程度、点鼻剤、洗眼剤またはコンタクトレンズ用剤の場合は、0.0005〜0.01w/v%、好ましくは0.001〜0.005w/v%程度、シロップ剤の場合は、0.01〜0.1w/v%、好ましくは0.01〜0.05w/v%である。
また、固形組成物の場合、4〜50重量%、好ましくは8〜45重量%である。具体的には、錠剤の場合は、1錠(100〜250mg)あたり1〜50mg、好ましくは2〜45mg程度で前記の重量%に含まれる範囲であればよい。成人一日服用量では、例えば0.1〜10000mg、好ましくは1〜1000mg程度に含まれる範囲であればよい。
In the composition of the present invention, the proportion of vitamin B 2 to be blended is not particularly limited as long as the effects of the present invention are obtained. For example, in the case of an aqueous composition, 0.0005 to 0.1 w / v%, preferably 0.001. It is about ~ 0.05w / v%. Specifically, in the case of eye drops, 0.005 to 0.1 w / v%, preferably about 0.01 to 0.05 w / v%, and in the case of nasal drops, eyewashes or contact lens agents, 0.0005 to 0.01 w / v. v%, preferably about 0.001 to 0.005 w / v%, and in the case of a syrup, it is 0.01 to 0.1 w / v%, preferably 0.01 to 0.05 w / v%.
Moreover, in the case of a solid composition, it is 4 to 50 weight%, Preferably it is 8 to 45 weight%. Specifically, in the case of a tablet, it may be in the range of 1 to 50 mg, preferably about 2 to 45 mg per tablet (100 to 250 mg) and included in the weight%. The daily dose for an adult may be within a range of, for example, about 0.1 to 10,000 mg, preferably about 1 to 1000 mg.
本発明の組成物において、プラノプロフェン又はその塩、およびビタミンB2類の配合比は、本発明の効果が得られれば特に制限はないが、プラノプロフェン又はその塩1重量部に対し、ビタミンB2類が0.001〜100重量部、好ましくは0.05〜10重量部、特に好ましくは0.2〜5重量部である。 In the composition of the present invention, the compounding ratio of pranoprofen or a salt thereof and vitamin B 2 is not particularly limited as long as the effect of the present invention is obtained, but with respect to 1 part by weight of pranoprofen or a salt thereof, Vitamin B 2 is 0.001 to 100 parts by weight, preferably 0.05 to 10 parts by weight, particularly preferably 0.2 to 5 parts by weight.
本発明の組成物には、目の疲れに対する改善効果を向上させるために、さらにモノテルペノイドを配合することができる。
モノテルペノイドとしては、メントール、カンフル、ボルネオール、リモネン、シネオール、テルピネン、フェランドレン、メントン、テルピネオール、カルボン、ペリルアルデヒド、チモール、p-シメン、カルバクロール、クミナール、ピネン、カンフェン、ツヨン、カレンなどの環状モノテルペノイド、ゲラニオール、ネロール、リナロール、シトラール、シトロネロール、シトロネラール、ミルセン、オシメンなどの鎖状モノテルペノイドが挙げられ、好ましくはメントール、カンフル、ボルネオール、リモネン、シネオール、ゲラニオール、リナロールである。これらのモノテルペノイドの立体構造は、d体、l体又はdl体、もしくは、(+)体、(−)体又は(±)体のいずれでも良い。これらの中で好ましくは、d-メントール、l-メントール、dl-メントール、d-カンフル、dl-カンフル、d-ボルネオール、dl-ボルネオール、d-リモネン、l-リモネン、dl-リモネン、d-リナロール、l-リナロールであり、特に好ましくは、l-メントール、d-カンフル、d-ボルネオールである。
また、モノテルペノイドは精油等の混合物として配合しても良く、例えば、ユーカリ油、ベルガモット油、ペパーミント油、クールミント油、スペアミント油、ハッカ油、ヒノキ油、テレビン油、スギ油、樟脳油、クロモジ油、バラ油、ゲラニウム油、レモン油、オレンジ油、橙皮油、サンショウ油、タイム油、ラベンダー油、シトロネラ油、レモングラス油、ユーカリ油、ハッカ水などが挙げられる。
これらのモノテルペノイドは、1種単独で使用してもよく、また2種以上を任意に組み合わせて使用してもよい。
本発明の組成物において、配合するモノテルペノイドの割合は、例えば、水性組成物の場合、0.00005〜5w/v%、好ましくは0.0001〜1w/v%、特に好ましくは0.0002〜0.1w/v%が例示される。
The composition of the present invention may further contain a monoterpenoid in order to improve the effect of improving eye fatigue.
Monoterpenoids include cyclic groups such as menthol, camphor, borneol, limonene, cineol, terpinene, ferrandrene, menthone, terpineol, carvone, perylaldehyde, thymol, p-cymene, carvacrol, cuminal, pinene, camphene, tuyon, and karen. Examples thereof include chain monoterpenoids such as monoterpenoid, geraniol, nerol, linalool, citral, citronellol, citronellal, myrcene and ocimene, and menthol, camphor, borneol, limonene, cineol, geraniol and linalool are preferred. The three-dimensional structure of these monoterpenoids may be d-form, l-form or dl-form, or (+)-form, (-)-form or (±) -form. Among these, d-menthol, l-menthol, dl-menthol, d-camphor, dl-camphor, d-borneol, dl-borneol, d-limonene, l-limonene, dl-limonene, d-linalool L-linalool, particularly preferably l-menthol, d-camphor and d-borneol.
Monoterpenoids may be blended as a mixture of essential oils, such as eucalyptus oil, bergamot oil, peppermint oil, cool mint oil, spearmint oil, mint oil, cypress oil, turpentine oil, cedar oil, camphor oil, chromodi oil. , Rose oil, geranium oil, lemon oil, orange oil, orange peel oil, salamander oil, thyme oil, lavender oil, citronella oil, lemongrass oil, eucalyptus oil, peppermint water and the like.
These monoterpenoids may be used alone or in any combination of two or more.
In the composition of the present invention, the proportion of the monoterpenoid to be blended is, for example, 0.00005 to 5 w / v%, preferably 0.0001 to 1 w / v%, particularly preferably 0.0002 to 0.1 w / v% in the case of an aqueous composition. Illustrated.
本発明の組成物には、本発明の製剤の安定性を増強又は補足する目的で、さらに粘稠剤、キレート剤、非イオン性界面活性剤、防腐剤、緩衝剤、pH調整剤を1種または2種以上組み合わせて配合することができる。 In the composition of the present invention, for the purpose of enhancing or supplementing the stability of the preparation of the present invention, a thickener, chelating agent, nonionic surfactant, preservative, buffer, and pH adjuster Or it can mix | blend in combination of 2 or more types.
粘稠剤としては、例えば、ポリビニルアルコール(完全又は部分ケン化物)、ポリビニルピロリドン(K25,K30,K90など)、カルボキシビニルポリマー、ポリオキシエチレン−ポリオキシプロピレンブロックコポリマー(BASF Wyandotte Coproration,プルロニック,テトロニックなど)、セルロース誘導体[メチルセルロース、エチルセルロース、ヒドロキシエチルセルロース、ヒドロキシプロピルセルロース、ヒドロキシプロピルメチルセルロース(2208,2906,2910など)、カルボキシメチルセルロース、カルボキシエチルセルロース、ニトロセルロース又はそれらの塩など]、マクロゴール(300,400,1500,4000など)、コンドロイチン硫酸ナトリウム、アラビアゴム、トラガント、デキストラン70、ブドウ糖、ソルビトールなどが例示でき、好ましくはポリビニルアルコール(完全又は部分ケン化物)、ポリビニルピロリドン(K25,K30,K90など)、セルロース誘導体(メチルセルロース、ヒドロキシエチルセルロース、ヒドロキシプロピルセルロース、ヒドロキシプロピルメチルセルロース(2208,2906,2910など)、カルボキシメチルセルロース又はそれらの塩)、マクロゴール300、マクロゴール400、デキストラン70である。
これらの粘稠剤は、1種単独で使用してもよく、また2種以上を任意に組み合わせて使用してもよい。
本発明の組成物において、配合する粘稠剤の割合は、例えば、水性組成物の場合、0.0005〜5w/v%が例示される。
Examples of the thickener include polyvinyl alcohol (completely or partially saponified), polyvinylpyrrolidone (K25, K30, K90, etc.), carboxyvinyl polymer, polyoxyethylene-polyoxypropylene block copolymer (BASF Wyandotte Coproration, Pluronic, Tronic, etc.), cellulose derivatives [methylcellulose, ethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose (2208,2906,2910 etc.), carboxymethylcellulose, carboxyethylcellulose, nitrocellulose or their salts], macrogol (300,400, 1500,4000, etc.), chondroitin sodium sulfate, gum arabic, tragacanth, dextran 70, glucose, sorbitol, etc. Alcohol (completely or partially saponified), polyvinylpyrrolidone (K25, K30, K90, etc.), cellulose derivatives (methylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose (2208,2906,2910, etc.), carboxymethylcellulose or their Salt), Macrogol 300, Macrogol 400, and Dextran 70.
These thickening agents may be used alone or in any combination of two or more.
In the composition of the present invention, for example, in the case of an aqueous composition, the proportion of the thickening agent to be blended is 0.0005 to 5 w / v%.
キレート剤としては、エチレンジアミン四酢酸、アスコルビン酸、クエン酸、フィチン酸、ポリリン酸、メタリン酸、コハク酸又はそれらの塩等が挙げられる。これらの中で、好ましくはエチレンジアミン四酢酸、クエン酸又はそれらの塩、特に好ましくはエチレンジアミン四酢酸又はその塩である。
エチレンジアミン四酢酸の塩としては、医薬上、薬理学的に又は生理学的に許容されるものであれば、特に制限されず、例えばエチレンジアミン四酢酸ナトリウム、エチレンジアミン四酢酸二ナトリウム、エチレンジアミン四酢酸四ナトリウム等のアルカリ金属塩を挙げることができる。
エチレンジアミン四酢酸又はその塩は、水和物の形態で使用することもできる。水和物の形態のものとして、具体的には、エチレンジアミン四酢酸二ナトリウムの2水和物(以下、エデト酸ナトリウムとも言う)が例示できる。
これらのキレート剤は、1種単独で使用してもよく、また2種以上を任意に組み合わせて使用してもよい。
Examples of the chelating agent include ethylenediaminetetraacetic acid, ascorbic acid, citric acid, phytic acid, polyphosphoric acid, metaphosphoric acid, succinic acid, and salts thereof. Among these, ethylenediaminetetraacetic acid, citric acid or a salt thereof is preferable, and ethylenediaminetetraacetic acid or a salt thereof is particularly preferable.
The salt of ethylenediaminetetraacetic acid is not particularly limited as long as it is pharmaceutically, pharmacologically or physiologically acceptable. For example, sodium ethylenediaminetetraacetate, disodium ethylenediaminetetraacetate, tetrasodium ethylenediaminetetraacetate, etc. The alkali metal salt of can be mentioned.
Ethylenediaminetetraacetic acid or a salt thereof can also be used in the form of a hydrate. Specific examples of the hydrate form include disodium ethylenediaminetetraacetate (hereinafter also referred to as sodium edetate).
These chelating agents may be used alone or in any combination of two or more.
本発明の組成物において、配合するキレート剤の割合は、例えば、水性組成物の場合、0.0005〜0.5w/v%、好ましくは0.001〜0.2w/v%、更に好ましくは0.004〜0.1w/v%、特に好ましくは0.01〜0.05w/v%が例示される。 In the composition of the present invention, the ratio of the chelating agent to be added is, for example, 0.0005 to 0.5 w / v%, preferably 0.001 to 0.2 w / v%, more preferably 0.004 to 0.1 w / v in the case of an aqueous composition. %, Particularly preferably 0.01 to 0.05 w / v%.
非イオン性界面活性剤としては、医薬上、薬理学的に又は生理学的に許容されるものであれば、特に制限されない。例えば、ポリオキシエチレン(POE)−ポリオキシプロピレン(POP)ブロックコポリマー(例えば、ポロクサマー407、ポロクサマー235、ポロクサマー188など);エチレンジアミンのポリオキシエチレン-ポリオキシプロピレンブロックコポリマー付加物(例えば、ポロキサミン);モノラウリル酸POE(20)ソルビタン(ポリソルベート20)、モノオレイン酸POE(20)ソルビタン(ポリソルベート80)、ポリソルベート60等のPOEソルビタン脂肪酸エステル類;POE(60)硬化ヒマシ油等のPOE硬化ヒマシ油;POE(9)ラウリルエーテル等のPOEアルキルエーテル類;POE(20)POP(4)セチルエーテル等のPOE・POPアルキルエーテル類;POE(10)ノニルフェニルエーテル等のPOEアルキルフェニルエーテル類;POE(10)ノニルフェニルエーテル等のPOEアルキルフェニルエーテル類等が挙げられる。これらの中で、好ましくはポロクサマー407、ポリソルベート80、POE(60)硬化ヒマシ油、特に好ましくはポリソルベート80である。なお、括弧内の数字は付加モル数を示す。
これらの非イオン性界面活性剤は、1種単独で使用してもよく、また2種以上を任意に組み合わせて使用してもよい。
The nonionic surfactant is not particularly limited as long as it is pharmaceutically, pharmacologically or physiologically acceptable. For example, polyoxyethylene (POE) -polyoxypropylene (POP) block copolymers (eg, poloxamer 407, poloxamer 235, poloxamer 188, etc.); polyoxyethylene-polyoxypropylene block copolymer adducts of ethylenediamine (eg, poloxamine); POE sorbitan fatty acid esters such as monolauric acid POE (20) sorbitan (polysorbate 20), monooleic acid POE (20) sorbitan (polysorbate 80), polysorbate 60; POE cured castor oil such as POE (60) cured castor oil; POE (9) POE alkyl ethers such as lauryl ether; POE (20) POP (4) POE alkyl ethers such as cetyl ether; POE (10) POE alkyl phenyl ethers such as nonyl phenyl ether; POE (10 ) POE alkylphenyl ethers such as nonylphenyl ether . Of these, poloxamer 407, polysorbate 80, POE (60) hydrogenated castor oil, particularly preferably polysorbate 80 are preferred. The numbers in parentheses indicate the number of added moles.
These nonionic surfactants may be used alone or in any combination of two or more.
本発明の組成物において、配合する非イオン性界面活性剤の割合は、例えば、水性組成物の場合、0.001〜2w/v%、好ましくは0.01〜2w/v%、更に好ましくは0.05〜1w/v%、特に好ましくは0.15〜0.5w/v%が例示される。 In the composition of the present invention, the ratio of the nonionic surfactant to be blended is, for example, 0.001 to 2 w / v%, preferably 0.01 to 2 w / v%, more preferably 0.05 to 1 w / w in the case of an aqueous composition. Examples are v%, particularly preferably 0.15 to 0.5 w / v%.
防腐剤としては、ソルビン酸又はその塩、塩酸アルキルジアミノエチルグリシン、安息香酸ナトリウム、エタノール、塩化ベンザルコニウム、塩化ベンゼトニウム、グルコン酸クロルヘキシジン、クロロブタノール、デヒドロ酢酸ナトリウム、パラオキシ安息香酸メチル、パラオキシ安息香酸エチル、パラオキシ安息香酸プロピル、パラオキシ安息香酸ブチル、硫酸オキシキノリン、フェネチルアルコール、ベンジルアルコール、ビグアニド化合物(具体的には、ポリヘキサメチレンビグアニドなど)、グローキル(ローディア社製 商品名)等が挙げられる。これらの中で、好ましくはソルビン酸又はその塩、塩化ベンザルコニウム、塩酸アルキルジアミノエチルグリシン、特に好ましくはソルビン酸又はその塩である。
ソルビン酸の塩としては、例えば、無機塩基との塩[例えばアンモニウム塩;アルカリ金属塩(ナトリウム塩、カリウム塩など)、アルカリ土類金属塩(カルシウム塩、マグネシウム塩など)、アルミニウム塩等の金属との塩]、有機塩基との塩(例えば、メチルアミン、トリエチルアミン、ジエチルアミン、トリエタノールアミン、モルホリン、ピペラジン、ピロリジン、トリピリジン、ピコリン等の有機塩基との塩)等が例示され、特にナトリウム塩、カリウム塩が好ましい。
これらの防腐剤は、1種単独で使用してもよく、また2種以上を任意に組み合わせて使用してもよい。
Preservatives include sorbic acid or salts thereof, alkyldiaminoethylglycine hydrochloride, sodium benzoate, ethanol, benzalkonium chloride, benzethonium chloride, chlorhexidine gluconate, chlorobutanol, sodium dehydroacetate, methyl parahydroxybenzoate, paraoxybenzoic acid Examples thereof include ethyl, propyl paraoxybenzoate, butyl paraoxybenzoate, oxyquinoline sulfate, phenethyl alcohol, benzyl alcohol, biguanide compounds (specifically, polyhexamethylene biguanide, etc.), glow kill (trade name, manufactured by Rhodia), and the like. Of these, sorbic acid or a salt thereof, benzalkonium chloride, alkyldiaminoethylglycine hydrochloride, particularly preferably sorbic acid or a salt thereof.
Examples of sorbic acid salts include salts with inorganic bases [for example, ammonium salts; alkali metal salts (sodium salts, potassium salts, etc.), alkaline earth metal salts (calcium salts, magnesium salts, etc.), and aluminum salts. And salts with organic bases (for example, salts with organic bases such as methylamine, triethylamine, diethylamine, triethanolamine, morpholine, piperazine, pyrrolidine, tripyridine, picoline, etc.), particularly sodium salts, A potassium salt is preferred.
These preservatives may be used alone or in any combination of two or more.
本発明の組成物において、配合する防腐剤の割合は、例えば、水性組成物の場合、0.001〜2w/v%、好ましくは0.005〜0.5w/v%、更に好ましくは0.005〜0.3w/v%、特に好ましくは0.01〜0.2w/v%が例示される。 In the composition of the present invention, the proportion of the preservative to be added is, for example, 0.001 to 2 w / v%, preferably 0.005 to 0.5 w / v%, more preferably 0.005 to 0.3 w / v% in the case of an aqueous composition. Particularly preferably, 0.01 to 0.2 w / v% is exemplified.
緩衝剤としては、ホウ酸緩衝剤、リン酸緩衝剤、炭酸緩衝剤、クエン酸緩衝剤、酢酸緩衝剤、イプシロン−アミノカプロン酸、アミノエチルスルホン酸、アスパラギン酸、アスパラギン酸塩などが挙げられる。これらの中で、好ましくはホウ酸緩衝剤、リン酸緩衝剤であり、特に好ましくはホウ酸緩衝剤である。
ホウ酸緩衝剤の具体例として、ホウ酸及びその塩(ホウ酸ナトリウム、テトラホウ酸カリウム、メタホウ酸カリウム、ホウ酸アンモニウム、ホウ砂など)が例示され、特に、ホウ酸、ホウ砂が好ましい。
リン酸緩衝剤、炭酸緩衝剤、クエン酸緩衝剤、酢酸緩衝剤の具体例として、クエン酸、クエン酸ナトリウム、酢酸、酢酸カリウム、酢酸ナトリウム、炭酸水素ナトリウム、炭酸ナトリウム、ホウ酸、ホウ砂、リン酸水素二ナトリウム、リン酸二水素ナトリウム、リン酸二水素カリウムなどが例示される。
Examples of the buffer include borate buffer, phosphate buffer, carbonate buffer, citrate buffer, acetate buffer, epsilon-aminocaproic acid, aminoethylsulfonic acid, aspartic acid, aspartate and the like. Among these, a borate buffer and a phosphate buffer are preferable, and a borate buffer is particularly preferable.
Specific examples of the boric acid buffer include boric acid and salts thereof (sodium borate, potassium tetraborate, potassium metaborate, ammonium borate, borax, etc.), and boric acid and borax are particularly preferable.
Specific examples of phosphate buffer, carbonate buffer, citrate buffer, and acetate buffer include citric acid, sodium citrate, acetic acid, potassium acetate, sodium acetate, sodium bicarbonate, sodium carbonate, boric acid, borax, Examples thereof include disodium hydrogen phosphate, sodium dihydrogen phosphate, potassium dihydrogen phosphate and the like.
本発明の組成物において、配合する緩衝剤の割合は、使用する緩衝剤の種類や期待される効果等に応じて異なり、一律に規定することはできないが、例えば、水性組成物の場合、0.01〜3w/v%、好ましくは0.1〜2w/v%、更に好ましくは0.3〜2w/v%、特に好ましくは0.5〜2w/v%が例示される。 In the composition of the present invention, the ratio of the buffering agent to be blended varies depending on the type of buffering agent used and the expected effect and cannot be uniformly defined.For example, in the case of an aqueous composition, 0.01% -3 w / v%, preferably 0.1-2 w / v%, more preferably 0.3-2 w / v%, particularly preferably 0.5-2 w / v%.
pH調整剤としては、塩酸、ホウ酸、アミノエチルスルホン酸、イプシロン−アミノカプロン酸、酢酸、水酸化ナトリウム、炭酸水素ナトリウム、炭酸ナトリウム、ホウ砂、トリエタノールアミン、モノエタノールアミンなどが挙げられる。これらの中で、特に好ましくは塩酸、水酸化ナトリウムである。 Examples of the pH adjuster include hydrochloric acid, boric acid, aminoethylsulfonic acid, epsilon-aminocaproic acid, acetic acid, sodium hydroxide, sodium hydrogen carbonate, sodium carbonate, borax, triethanolamine, monoethanolamine and the like. Of these, hydrochloric acid and sodium hydroxide are particularly preferred.
本発明の組成物において、適切なpHは水性組成物の適用部位、剤形等により異なるが、通常6.0〜9.0、好ましくは6.5〜8.5、更に好ましくは6.8〜8.2、特に好ましくは7.0〜8.0程度である。これらの範囲内から著しく逸脱すると、プラノプロフェンまたはその塩の化学的安定性が低下する可能性があり、また生体に許容されないため、好ましくない。
pH調整は、前記緩衝剤、pH調整剤等を用いて、当該技術分野で既知の方法で行うことができる。
In the composition of the present invention, the appropriate pH varies depending on the application site, dosage form and the like of the aqueous composition, but is usually 6.0 to 9.0, preferably 6.5 to 8.5, more preferably 6.8 to 8.2, particularly preferably about 7.0 to 8.0. It is. A significant deviation from these ranges is undesirable because it may reduce the chemical stability of pranoprofen or a salt thereof and is not acceptable to the living body.
The pH adjustment can be performed by a method known in the art using the buffer, the pH adjuster, or the like.
本発明の組成物は、目の疲れを改善するために、局所投与または全身投与して用いることができる。本発明はプラノプロフェンまたはその塩とビタミン類が共存することで効果が奏されるため、投与後に作用部位でより協同しやすい局所投与であることが好ましい。また、作用部位において速やかに効果を発揮しやすい水性組成物であることが望ましい。 The composition of the present invention can be used locally or systemically to improve eye fatigue. Since the effect of the present invention is exhibited by the coexistence of pranoprofen or a salt thereof and vitamins, it is preferable that the administration be local administration that facilitates cooperation at the site of action after administration. Moreover, it is desirable that it is an aqueous composition which tends to exhibit an effect quickly in an action site.
本発明の組成物は、特定の形態に限定されず、目的に応じて、液剤、半固形剤あるいは固形剤(固形組成物)、好ましくは液剤あるいは固形剤をあげることができる。具体的には、液剤、半固形剤(軟膏剤)、錠剤(口腔内速崩解錠、咀嚼可能錠、有核錠、多層錠、発泡錠、トローチ剤、ゼリー状ドロップ剤などを含む)、顆粒剤、細粒剤、散剤、硬カプセル剤、軟カプセル剤、ゲル剤、ゼリー剤等を例示できる。
好ましくは液剤、錠剤、顆粒剤、硬カプセル剤または軟カプセル剤であり、特に好ましくは液剤である。
The composition of this invention is not limited to a specific form, According to the objective, a liquid agent, a semisolid agent, or a solid agent (solid composition), Preferably a liquid agent or a solid agent can be mention | raise | lifted. Specifically, liquids, semi-solid preparations (ointments), tablets (including intraoral quick disintegrating tablets, chewable tablets, dry tablets, multilayer tablets, effervescent tablets, lozenges, jelly-like drops, etc.), Examples thereof include granules, fine granules, powders, hard capsules, soft capsules, gels, and jelly agents.
A liquid, tablet, granule, hard capsule or soft capsule is preferable, and a liquid is particularly preferable.
液剤としては、均一溶液であっても懸濁液であっても、混合又は溶解して使用する組成物であっても良い。具体的には、点眼剤(液)[但し、点眼剤にはコンタクトレンズ装用中に点眼可能な点眼剤(液)を含む]、洗眼剤(液)[但し、洗眼剤にはコンタクトレンズ装用中に洗眼可能な洗眼剤(液)を含む]、点鼻剤(液)、コンタクトレンズ用剤[コンタクトレンズ装着液、コンタクトレンズケア用剤(コンタクトレンズ消毒剤、コンタクトレンズ用保存剤、コンタクトレンズ用洗浄剤、コンタクトレンズ用洗浄保存剤)等]、シロップ剤、ドリンク剤等を挙げることができる。これらの中で、好ましくは局所投与用である、点眼剤、洗眼剤、点鼻剤、コンタクトレンズ用剤であり、更に好ましくは点眼剤、洗眼剤、コンタクトレンズ用剤などの眼科用組成物である。
前記コンタクトレンズ用剤は、ハードコンタクトレンズ、ソフトコンタクトレンズを含むあらゆるコンタクトレンズに適用できるが、特に目が疲れやすいと言われるソフトコンタクトレンズに適用することが好ましい。
これらの製剤は常法により調製して得られ、その際、上述の成分に加えてその製剤に応じた慣用の添加剤を使用することができる。
The liquid agent may be a uniform solution, a suspension, or a composition used by mixing or dissolving. Specifically, eye drops (liquid) [however, eye drops include eye drops (liquid) that can be applied while wearing contact lenses], eye wash (liquid) [however, eye drops are used when wearing contact lenses. Eyewash (liquid), nasal drops (liquid), contact lens preparation [contact lens mounting liquid, contact lens care preparation (contact lens disinfectant, contact lens preservative, contact lens use] Cleaning agents, contact lens cleaning preservatives etc.)], syrups, drinks and the like. Among these, an ophthalmic composition, preferably an eye drop, an eye wash, a nasal drop, and a contact lens preparation for topical administration, and more preferably an ophthalmic composition such as an eye drop, eye wash, contact lens preparation, etc. is there.
The contact lens agent can be applied to all contact lenses including hard contact lenses and soft contact lenses, but is particularly preferably applied to soft contact lenses said to be prone to eye fatigue.
These preparations are obtained by a conventional method, and in this case, in addition to the above-mentioned components, conventional additives corresponding to the preparation can be used.
本発明の組成物の用途としては、プラノプロフェンおよびビタミンB2の本来有する薬理作用に基づく抗炎症、代謝障害改善などのほか、目の疲れの改善が挙げられる。本発明の組成物のうち、点眼剤または洗眼剤が、目の疲れ改善用に好適である。 The use of the composition of the present invention, an anti-inflammatory based on pharmacological effects inherent in pranoprofen and vitamin B 2, addition, metabolic disorder improving include improvement of eye fatigue. Of the compositions of the present invention, eye drops or eye washes are suitable for improving eye fatigue.
本発明の組成物は、340nm〜380nmの吸光度が1.0以上である容器に収容されていると、プラノプロフェンをより安定化できるため好ましい。340nm〜380nmの吸光度が1.0以上である容器とは、340 nm、350 nm、360 nm、370 nm、380 nmの吸光度の平均が1.0以上である容器である。好ましくは2.0以上、さらに好ましくは2.5以上、特に好ましくは3.0以上、さらに特に好ましくは3.5以上であるとよい。 The composition of the present invention is preferably contained in a container having an absorbance of 340 nm to 380 nm of 1.0 or more because pranoprofen can be further stabilized. A container having an absorbance of 340 nm to 380 nm of 1.0 or more is a container having an average absorbance of 340 nm, 350 nm, 360 nm, 370 nm, and 380 nm of 1.0 or more. It is preferably 2.0 or more, more preferably 2.5 or more, particularly preferably 3.0 or more, and still more preferably 3.5 or more.
本発明の水性組成物を収容する容器において吸光度は、第十四改正日本薬局方「プラスチック製医薬品容器試験法 4.透明性試験」に準じて、次の方法により測定する。
容器胴部からできるだけ湾曲が少なく厚さが均一な部分をとって、縦2〜4cm、横0.9〜1.1cmの大きさに切断したもの5個を、それぞれ水を満たした紫外線吸光スペクトル測定用セルに浸し、水だけを満たしたセルを対照として、各測定波長について紫外可視吸光度測定法により吸光度を測定する。
The absorbance in the container containing the aqueous composition of the present invention is measured by the following method according to the 14th revised Japanese Pharmacopoeia “Plastic drug container test method 4. Transparency test”.
UV absorption spectrum measurement cells filled with water, each of 5 pieces cut to a size of 2 to 4 cm in length and 0.9 to 1.1 cm in width, taking a portion with as little curvature as possible from the container body. Absorbance is measured by the UV-visible absorbance measurement method for each measurement wavelength, using a cell immersed in water and filled with water alone as a control.
本発明の水性組成物を収容する容器は、例えば、プラスチック容器又はガラス容器等のうち、前述の吸光度が達成されているものであれば用いることができる。
プラスチック容器の材質としては、例えば、オレフィン系樹脂(ポリエチレン、ポリプロピレンなど)、ポリエチレンテレフタレート系樹脂、ポリエチレンナフタレート系樹脂、ポリアリレート系樹脂、ポリエステル系樹脂、ポリフェニレンエーテル系樹脂、ポリカーボネート系樹脂、ポリスルホン系樹脂、ポリアミド系樹脂、硬質塩化ビニル樹脂、スチレン系樹脂(ポリスチレン、アクリロニトリル−スチレン共重合体(AS樹脂)など)、セルロースアセテート類などの合成樹脂が例示でき、プラスチック容器を構成する主原料として、好ましくは、オレフィン系樹脂又はポリエステル系樹脂である。なお、「主原料」とは、プラスチック容器の全構成原料の内、50重量%以上、好ましくは70重量%以上を占める原料を示す。
The container for storing the aqueous composition of the present invention can be used as long as the aforementioned absorbance is achieved, for example, among plastic containers or glass containers.
Examples of plastic container materials include olefin resins (polyethylene, polypropylene, etc.), polyethylene terephthalate resins, polyethylene naphthalate resins, polyarylate resins, polyester resins, polyphenylene ether resins, polycarbonate resins, polysulfone resins. Resin, polyamide resin, hard vinyl chloride resin, styrene resin (polystyrene, acrylonitrile-styrene copolymer (AS resin), etc.), synthetic resins such as cellulose acetate can be exemplified, and as a main raw material constituting a plastic container, An olefin resin or a polyester resin is preferable. The “main raw material” refers to a raw material that occupies 50% by weight or more, preferably 70% by weight or more, of all constituent raw materials of the plastic container.
本発明の水性組成物を収容する容器のうち、プラスチック容器を構成する主原料として好ましくは、ポリエチレンナフタレート、ポリアリレート、ポリエチレンテレフタレート、ポリプロピレン、ポリエチレンのいずれか1種、これらの共重合ポリエステル、または2種以上の混合体が挙げられる。
共重合ポリエステルとしては、エチレン−2,6−ナフタレート単位、アリレート単位、エチレンテレフタレート単位、プロピレン単位、エチレン単位のいずれか1種を主体として、他のポリエステル単位を含む共重合ポリエステルであり、共重合酸成分の例としては例えば、テレフタル酸、イソフタル酸、ヘキサヒドロテレフタル酸、ナフタレン−2,6−ジカルボン酸、アジピン酸等があり、共重合グリコール成分の例としては例えば、1,3−プロパンジオール、テトラメチレングリコール、1,4−シクロヘキサンジメタノール、ネオペンチルグリコール、プロピレングリコール、1,4−ブタンジオール、ジエチレングリコールなどが挙げられる。
Of the containers containing the aqueous composition of the present invention, the main raw material constituting the plastic container is preferably polyethylene naphthalate, polyarylate, polyethylene terephthalate, polypropylene, polyethylene, a copolymer polyester thereof, or 2 or more types of mixtures are mentioned.
The copolyester is a copolyester mainly comprising any one of ethylene-2,6-naphthalate unit, arylate unit, ethylene terephthalate unit, propylene unit, and ethylene unit, and other polyester units. Examples of the acid component include terephthalic acid, isophthalic acid, hexahydroterephthalic acid, naphthalene-2,6-dicarboxylic acid, and adipic acid. Examples of the copolymer glycol component include 1,3-propanediol. , Tetramethylene glycol, 1,4-cyclohexanedimethanol, neopentyl glycol, propylene glycol, 1,4-butanediol, diethylene glycol and the like.
本発明の水性組成物を収容する容器のうち、プラスチック容器として特に好ましくは、次の3種類の容器が挙げられる。
第一に、ポリエチレンナフタレート、ポリアリレートまたはこれらの共重合ポリエステルを主原料として構成される容器、第二に、ポリエチレンナフタレートまたはポリアリレートのいずれか1種以上とポリエチレンテレフタレート、ポリプロピレン、ポリエチレンのいずれか1種以上の混合体を主原料として構成された容器が挙げられ、好ましくはポリエチレンナフタレートとポリエチレンテレフタレートの混合体を主原料として構成された容器、第三に、ポリエチレンナフタレート、ポリアリレート、これらの共重合ポリエステル、ポリエチレンテレフタレート、ポリプロピレン、ポリエチレンから選択される1種、または2種以上の混合体を主原料として、紫外線遮断剤を添加またはコーティングした材質で構成された容器が挙げられる。紫外線遮断剤については後述の通りである。
Among the containers for storing the aqueous composition of the present invention, the following three kinds of containers are particularly preferable as plastic containers.
First, a container composed mainly of polyethylene naphthalate, polyarylate or a copolymer polyester thereof, and second, any one or more of polyethylene naphthalate or polyarylate and any of polyethylene terephthalate, polypropylene and polyethylene Or a container composed mainly of a mixture of at least one kind, preferably a container composed mainly of a mixture of polyethylene naphthalate and polyethylene terephthalate, and thirdly, polyethylene naphthalate, polyarylate, Containers made of a material obtained by adding or coating an ultraviolet blocking agent using one or a mixture of two or more selected from these copolymerized polyesters, polyethylene terephthalate, polypropylene, and polyethylene as main raw materials are listed. . The ultraviolet blocking agent is as described later.
本発明の水性組成物を収容する容器は、紫外線遮断剤を添加またはコーティングされた容器であっても良い。例えば、ガラスまたは合成樹脂などに紫外線遮断剤を添加した後に成型した容器、または合成樹脂などをシート状に加工してから紫外線遮断剤をコーティングしその後成型した容器、さらには、ガラスまたは合成樹脂などを最終容器形状に成型した後に紫外線遮断剤をコーティングした容器などが挙げられる。また、紫外線遮断剤を添加またはコーティングされたシート状合成樹脂などを、成型後の容器にシュリンク包装してもよい。 The container containing the aqueous composition of the present invention may be a container to which an ultraviolet blocking agent is added or coated. For example, a container molded after adding an ultraviolet blocking agent to glass or synthetic resin, or a container formed by processing a synthetic resin into a sheet and then coated with an ultraviolet blocking agent, and then molded, or glass or synthetic resin For example, a container coated with an ultraviolet blocking agent after being molded into a final container shape. Further, a sheet-like synthetic resin to which an ultraviolet blocking agent is added or coated may be shrink-wrapped in a molded container.
紫外線遮断剤としては、酸化亜鉛、酸化チタン、トリアゾール系化合物、ベンゾエート系化合物、置換アクリロニトリル系化合物、シアノアクリレート系化合物、トリアジン系化合物、シュウ酸アニリド系化合物、ニッケル錯体系化合物、商品名チヌビン(R)328、チヌビン(R)384-2、チヌビン(R)400、チヌビン(R)400-2、チヌビン(R)900、チヌビン(R)928、チヌビン(R)1130等のベンゾトリアゾール系化合物;ジイソプロピルケイ皮酸メチル、シノキサート、ジパラメトキシケイ皮酸モノ−2−エチルヘキサン酸グリセリル、パラメトキシケイ皮酸イソプロピル・ジイソプロピルケイ皮酸エステル混合物、パラメトキシケイ皮酸2−エチルヘキシル、ケイ皮酸ベンジル等のケイ皮酸系紫外線吸収剤;オキシベンゾン、ヒドロキシメトキシベンゾフェノンスルホン酸、ヒドロキシメトキシベンゾフェノンスルホン酸ナトリウム、ジヒドロキシジメトキシベンゾフェノン、ジヒドロキシジメトキシベンゾフェノンジスルホン酸ナトリウム、ジヒドロキシベンゾフェノン、テトラヒドロキシベンゾフェノン等のベンゾフェノン系紫外線吸収剤;パラアミノ安息香酸、パラアミノ安息香酸エチル、パラアミノ安息香酸グリセリル、パラジメチルアミノ安息香酸アミル、パラジメチルアミノ安息香酸2−エチルヘキシル、4−[N,N−ジ(2−ヒドロキシプロピル)アミノ]安息香酸エチル等の安息香酸エステル系紫外線吸収剤;サリチル酸エチレングリコール、サリチル酸オクチル、サリチル酸ジプロピレングリコール、サリチル酸フェニル、サリチル酸ホモメンチル、サリチル酸メチル等のサリチル酸系紫外線吸収剤、グアイアズレン、ジメトキシベンジリデンジオキソイミダゾリジンプロピオン酸2−エチルヘキシル、2,4,6−トリス[4−(2−エチルヘキシルオキシカルボニル)アニリノ]1,3,5−トリアジン、パラヒドロキシアニソール、2−(2−ヒドロキシ−5−メチルフェニル)ベンゾトリアゾール、4−tert−ブチル−4’−メトキシジベンゾイルメタン、フェニルベンズイミダゾールスルホン酸、2−(4−ジエチルアミノ−2−ヒドロキシベンゾイル)−安息香酸ヘキシルなどが挙げられる。また、リボフラビン、アントラキノン系色素(1−アミノ−4−メチルアントラキノン、1,4−ジアミノアントラキノン、アントラキノン系イエローなど)、フタロシアニン系色素(フタロシアニンブルー(C.I. Pigment Blue 15;C.I. 74160;青色404号)、フタロシアニングリーン(C.I. Pigment Green 7)など)など340nm〜380nmに吸収を有する着色剤であってもよい。
好ましくは酸化亜鉛、酸化チタン、チヌビン(R)328、チヌビン(R)384-2、チヌビン(R)400、チヌビン(R)400-2、チヌビン(R)900、チヌビン(R)928、チヌビン(R)1130、パラメトキシケイ皮酸2−エチルヘキシル、ジパラメトキシケイ皮酸モノ−2−エチルヘキサン酸グリセリル、2,4,6−トリス[4−(2−エチルヘキシルオキシカルボニル)アニリノ]1,3,5−トリアジン、フェニルベンズイミダゾールスルホン酸、2−(4−ジエチルアミノ−2−ヒドロキシベンゾイル)−安息香酸ヘキシル、ジメトキシベンジリデンジオキソイミダゾリジンプロピオン酸2−エチルヘキシルが挙げられ、特に好ましくは酸化亜鉛、酸化チタン、チヌビン(R)328、チヌビン(R)384-2、チヌビン(R)400、チヌビン(R)400-2、チヌビン(R)900、チヌビン(R)928、チヌビン(R)1130である。酸化亜鉛、酸化チタンはさらにシリカ、シリコン、ケイ酸亜鉛などで被覆されていてもよい。
As UV-blocking agents, zinc oxide, titanium oxide, triazole compounds, benzoate compounds, substituted acrylonitrile compounds, cyanoacrylate compounds, triazine compounds, oxalic anilide compounds, nickel complex compounds, trade name Tinuvin (R ) Benzotriazole compounds such as 328, Tinuvin (R) 384-2, Tinuvin (R) 400, Tinuvin (R) 400-2, Tinuvin (R) 900, Tinuvin (R) 928, Tinuvin (R) 1130; Methyl cinnamate, sinoxate, diparamethoxycinnamate mono-2-ethylhexanoate glyceryl, paramethoxycinnamate isopropyl diisopropylcinnamate mixture, paramethoxycinnamate 2-ethylhexyl, cinnamate benzyl, etc. Cinnamate UV absorbers; oxybenzone, hydroxymethoxybenzophenone sulfo Acid, sodium hydroxymethoxybenzophenonesulfonate, dihydroxydimethoxybenzophenone, dihydroxydimethoxybenzophenone sodium disulfonate, dihydroxybenzophenone, tetrahydroxybenzophenone and other benzophenone UV absorbers; paraaminobenzoic acid, ethyl paraaminobenzoate, glyceryl paraaminobenzoate, paradimethyl Benzoic acid ester UV absorbers such as amyl aminobenzoate, 2-ethylhexyl paradimethylaminobenzoate, ethyl 4- [N, N-di (2-hydroxypropyl) amino] benzoate; ethylene glycol salicylate, octyl salicylate, Salicylic acid UV such as dipropylene glycol salicylate, phenyl salicylate, homomenthyl salicylate, methyl salicylate Absorbent, guaiazulene, dimethoxybenzylidenedioxoimidazolidinepropionate 2-ethylhexyl, 2,4,6-tris [4- (2-ethylhexyloxycarbonyl) anilino] 1,3,5-triazine, parahydroxyanisole, 2- (2-hydroxy-5-methylphenyl) benzotriazole, 4-tert-butyl-4′-methoxydibenzoylmethane, phenylbenzimidazolesulfonic acid, 2- (4-diethylamino-2-hydroxybenzoyl) -benzoic acid hexyl, etc. Is mentioned. Riboflavin, anthraquinone dyes (1-amino-4-methylanthraquinone, 1,4-diaminoanthraquinone, anthraquinone yellow, etc.), phthalocyanine dyes (phthalocyanine blue (CI Pigment Blue 15; CI 74160; blue 404)), A colorant having absorption at 340 nm to 380 nm such as phthalocyanine green (CI Pigment Green 7) may be used.
Preferably zinc oxide, titanium oxide, Tinuvin (R) 328, Tinuvin (R) 384-2, Tinuvin (R) 400, Tinuvin (R) 400-2, Tinuvin (R) 900, Tinuvin (R) 928, Tinuvin ( R) 1130, 2-ethylhexyl paramethoxycinnamate, glyceryl mono-2-ethylhexanoate diparamethoxycinnamate, 2,4,6-tris [4- (2-ethylhexyloxycarbonyl) anilino] 1,3 , 5-triazine, phenylbenzimidazolesulfonic acid, 2- (4-diethylamino-2-hydroxybenzoyl) -benzoyl hexyl, dimethoxybenzylidenedioxoimidazolidinepropionate 2-ethylhexyl, particularly preferably zinc oxide, oxidation Titanium, Tinuvin (R) 328, Tinuvin (R) 384-2, Tinuvin (R) 400, Tinuvin (R) 400-2, Tinuvin (R) 900, Tinuvin (R) 928, Tinuvin (R) 1130 . Zinc oxide and titanium oxide may be further coated with silica, silicon, zinc silicate or the like.
具体的には、ポリエチレンに酸化亜鉛を添加またはコーティングされた容器、ポリプロピレンに酸化亜鉛を添加またはコーティングされた容器、ポリエチレンテレフタレートに酸化亜鉛を添加またはコーティングされた容器などが挙げられ、好ましくはポリエチレンテレフタレートに酸化亜鉛を添加またはコーティングされた容器である。
本発明の水性組成物を収容する容器において、添加する紫外線遮断剤の割合は、例えば、0.05〜5.0重量%、好ましくは0.1〜3.0重量%が例示される。
Specific examples include containers in which zinc oxide is added or coated on polyethylene, containers in which zinc oxide is added or coated on polypropylene, containers in which zinc oxide is added or coated on polyethylene terephthalate, and preferably polyethylene terephthalate. A container in which zinc oxide is added or coated.
In the container containing the aqueous composition of the present invention, the proportion of the ultraviolet blocking agent to be added is, for example, 0.05 to 5.0% by weight, preferably 0.1 to 3.0% by weight.
本発明の水性組成物を収容する容器において、紫外線遮断剤をコーティングされた容器は、例えば、紫外線吸収剤を含有するコーティング塗料を成型後の容器や合成樹脂シートなどに塗布することで製することができる。ここで、コーティング塗料としては、透明のものであって、ラジカル重合系のアクリル型(例えば、ポリエステルポリアクリレート、ウレタンポリアクリレート、エポキシポリアクリレート、ポリエーテルポリアクリレート、側鎖アクリロイル型アクリル樹脂等)、チオールエン型(例えば、ポリチオールアクリル型オリゴマー、ポリチオールスピロアセタール型等)、不飽和ポリエステル又はカチオン重合系のエポキシ樹脂等を用いることができる。 In the container containing the aqueous composition of the present invention, a container coated with an ultraviolet blocking agent is manufactured by, for example, applying a coating paint containing an ultraviolet absorber to a molded container or a synthetic resin sheet. Can do. Here, the coating paint is transparent and is a radical polymerization type acrylic type (for example, polyester polyacrylate, urethane polyacrylate, epoxy polyacrylate, polyether polyacrylate, side chain acryloyl type acrylic resin, etc.), Thiolene type (for example, polythiol acrylic type oligomer, polythiol spiroacetal type, etc.), unsaturated polyester, or cationic polymerization type epoxy resin can be used.
また、本発明の組成物を収容する容器は、容器を構成する素材をフィルム状に展延し、このフィルムを接着積層したシートから成型したものであってもよい。
また、内容物の異物試験または残存容量確認ができることなどから、450nmの吸光度が1.0以下、好ましくは0.8以下、さらに好ましくは0.6以下、特に好ましくは0.4以下、さらに特に好ましくは0.2以下であるとよい。
Moreover, the container which accommodates the composition of this invention may shape | mold from the sheet | seat which extended the raw material which comprises a container in the shape of a film, and adhere | attached and laminated | stacked this film.
In addition, the absorbance at 450 nm is 1.0 or less, preferably 0.8 or less, more preferably 0.6 or less, particularly preferably 0.4 or less, and still more preferably 0.2 or less, because the foreign matter test of the contents or confirmation of the remaining capacity can be performed. .
本発明の組成物は、必要に応じて、浸透圧比を生体に許容される範囲内に調整することができる。適切な浸透圧比は、水性組成物の適用部位、剤形等により異なるが、通常0.3〜4.2、好ましくは0.3〜2.1、さらに好ましくは0.5〜1.8、特に好ましくは0.6〜1.5程度である。浸透圧の調整は無機塩及び多価アルコール、糖アルコール、糖類などを用いて当該技術分野で既知の方法で行うことができる。 In the composition of the present invention, the osmotic pressure ratio can be adjusted within a range acceptable to a living body, if necessary. The appropriate osmotic pressure ratio varies depending on the application site, dosage form and the like of the aqueous composition, but is usually 0.3 to 4.2, preferably 0.3 to 2.1, more preferably 0.5 to 1.8, and particularly preferably about 0.6 to 1.5. The osmotic pressure can be adjusted by a method known in the art using an inorganic salt and a polyhydric alcohol, sugar alcohol, saccharide or the like.
浸透圧比は、第十四改正日本薬局方に基づき0.9w/v%塩化ナトリウム水溶液の浸透圧に対する試料の浸透圧の比とし、浸透圧は日本薬局方記載の浸透圧測定法(氷点降下法)を用いて測定する。浸透圧比測定用標準液は、塩化ナトリウム(日本薬局方標準試薬)を500〜650℃で40〜50分間乾燥した後、デシケーター(シリカゲル)中で放冷し、その0.900gを正確に量り、精製水に溶かし正確に100mLとして調製するか、市販の浸透圧比測定用標準液(0.9w/v%塩化ナトリウム水溶液)を用いる。 The osmotic pressure ratio is the ratio of the osmotic pressure of the sample to the osmotic pressure of 0.9 w / v% sodium chloride aqueous solution based on the 14th revised Japanese pharmacopoeia. Use to measure. The standard solution for measuring the osmotic pressure ratio was sodium chloride (Japanese Pharmacopoeia standard reagent) dried at 500-650 ° C for 40-50 minutes, then allowed to cool in a desiccator (silica gel), accurately weighed 0.900 g and purified. Dissolve in water to make exactly 100 mL, or use a commercially available standard solution for osmotic pressure ratio measurement (0.9 w / v% sodium chloride aqueous solution).
本発明の組成物は、本発明の効果を奏していれば、上記成分の他に、種々の成分(薬理活性成分や生理活性成分を含む)を組み合わせて含有することができる。このような成分の種類は特に制限されず、例えば、充血除去成分、眼筋調節薬成分、抗炎症薬成分または収斂薬成分、抗ヒスタミン薬成分又は抗アレルギー薬成分、ビタミン類、アミノ酸類、抗菌薬成分、殺菌薬成分、局所麻酔薬成分、ステロイド成分、緑内障治療成分、白内障治療成分、解熱鎮痛薬成分、鎮静催眠薬成分、鎮咳薬成分、気管支拡張薬成分または交感神経興奮薬成分、去痰薬成分、生薬成分などが例示できる。本発明において好適な成分としては、例えば、次のような成分が挙げられる。 The composition of the present invention can contain various components (including pharmacologically active components and physiologically active components) in combination with the above components as long as the effects of the present invention are exhibited. The type of such component is not particularly limited, and examples thereof include a decongestant component, an ocular muscle modulator component, an anti-inflammatory component or an astringent component, an antihistamine component or an antiallergic component, vitamins, amino acids, antibacterial agents. Drug component, bactericidal component, local anesthetic component, steroid component, glaucoma treatment component, cataract treatment component, antipyretic analgesic component, sedative hypnotic component, antitussive component, bronchodilator component or sympathomimetic component, expectorant Ingredients, herbal medicine ingredients and the like can be exemplified. Examples of suitable components in the present invention include the following components.
充血除去成分:例えば、α−アドレナリン作動薬、具体的にはエピネフリン、塩酸エピネフリン、塩酸エフェドリン、塩酸オキシメタゾリン、塩酸テトラヒドロゾリン、塩酸ナファゾリン、塩酸フェニレフリン、塩酸メチルエフェドリン、酒石酸水素エピネフリン、硝酸ナファゾリンなど。これらはd体、l体又はdl体のいずれでもよい。 Decongestant: For example, α-adrenergic agonists, specifically epinephrine, epinephrine hydrochloride, ephedrine hydrochloride, oxymetazoline hydrochloride, tetrahydrozoline hydrochloride, naphazoline hydrochloride, phenylephrine hydrochloride, methylephedrine hydrochloride, epinephrine hydrogen tartrate, naphazoline nitrate. These may be d-form, l-form or dl-form.
眼筋調節薬成分:例えば、アセチルコリンと類似した活性中心を有するコリンエステラーゼ阻害剤、具体的にはメチル硫酸ネオスチグミン、トロピカミド、ヘレニエン硫酸アトロピンなど。 Eye muscle modulator component: For example, cholinesterase inhibitor having an active center similar to acetylcholine, specifically, neostigmine methyl sulfate, tropicamide, atropine sulfate helenien, and the like.
抗炎症薬成分または収斂薬成分:例えば、硫酸亜鉛、乳酸亜鉛、アラントイン、イプシロン−アミノカプロン酸、インドメタシン、塩化リゾチーム、硝酸銀、アズレンスルホン酸ナトリウム、グリチルリチン酸二カリウム、グリチルリチン酸アンモニウム、ジクロフェナクナトリウム、ブロムフェナクナトリウム、塩化ベルベリン、硫酸ベルベリン、ピロキシカムなど。 Anti-inflammatory component or astringent component: for example, zinc sulfate, zinc lactate, allantoin, epsilon-aminocaproic acid, indomethacin, lysozyme chloride, silver nitrate, sodium azulenesulfonate, dipotassium glycyrrhizinate, ammonium glycyrrhizinate, diclofenac sodium, bromfena Sodium chloride, berberine chloride, berberine sulfate, piroxicam, etc.
抗ヒスタミン薬成分又は抗アレルギー薬成分:例えば、アシタザノラスト、アンレキサノクス、イブジラスト、ペミロラスト、タザノラスト、トラニラスト、塩酸ジフェンヒドラミン、塩酸レボカバスチン、フマル酸ケトチフェン、クロモグリク酸ナトリウム、ペミロラストカリウム、マレイン酸クロルフェニラミン、イプロヘプチン、イソチペンジル、ジフェテロール、ジフェニルピラリン、トリプロリジン、トリペレナミン、トンジルアミン、プロメタジン、メトジラジン、カルビノキサミン、アリメマジン、プロメタジン、メブヒドロリン、フェネタジン、オキサトミド、メキタジン、テルフェナジン、エピナスチン、アステミゾール、エバスチン、セチリジン、オロパタジン、フマル酸エメダスチン、フマル酸クレマスチン、塩酸アゼラスチンなど。 Antihistamine component or antiallergic agent component: for example, agitazanolast, amlexanox, ibudilast, pemirolast, tazanolast, tranilast, diphenhydramine hydrochloride, levocabastine hydrochloride, ketotifen fumarate, sodium cromoglycate, potassium pemirolast, chlorpheniramine maleate , Iproheptin, isothipentyl, dipheterol, diphenylpyralin, triprolidine, tripelenamine, tondilamine, promethazine, methodirazine, carbinoxamine, alimemazine, promethazine, mebuhydrolin, phenetadine, oxatomide, mequitazine, terfenadine, epinastine, chinemethadine, rostemadine , Clemastine fumarate, hydrochloric acid Such as Rasuchin.
ビタミン類:例えば、酢酸レチノール、パルミチン酸レチノール、塩酸ピリドキシン、フラビンアデニンジヌクレオチドナトリウム、リン酸ピリドキサール、パンテノール、パントテン酸カルシウム、パントテン酸ナトリウム、アスコルビン酸、酢酸トコフェロールなど。 Vitamins: for example, retinol acetate, retinol palmitate, pyridoxine hydrochloride, sodium flavin adenine dinucleotide, pyridoxal phosphate, panthenol, calcium pantothenate, sodium pantothenate, ascorbic acid, tocopherol acetate.
アミノ酸類:例えば、アミノエチルスルホン酸(タウリン)、グルタミン酸、クレアチニン、アスパラギン酸カリウム、アスパラギン酸マグネシウム、アスパラギン酸マグネシウム・カリウム混合物、グルタミン酸ナトリウム、コンドロイチン硫酸ナトリウムなど。これらはd体、l体又はdl体のいずれでもよい。 Amino acids: For example, aminoethylsulfonic acid (taurine), glutamic acid, creatinine, potassium aspartate, magnesium aspartate, magnesium / aspartate mixture, sodium glutamate, sodium chondroitin sulfate and the like. These may be d-form, l-form or dl-form.
抗菌薬成分または殺菌薬成分:例えば、硫酸アミノデオキシカナマイシン、硫酸カナマイシン、硫酸ゲンタマイシン、硫酸シソマイシン、硫酸ストレプトマイシン、トブラマイシン、硫酸ミクロノマイシン、アルキルポリアミノエチルグリシン、クロラムフェニコール、スルファメトキサゾール、スルフイソキサゾール、スルファメトキサゾールナトリウム、スルフイソキサゾールジエタノールアミン、スルフイソキサゾールモノエタノールアミン、スルフイソメゾールナトリウム、スルフイソミジンナトリウム、塩酸テトラサイクリン、塩酸オキシテトラサイクリン、オフロキサシン、ノルフロキサシン、レボフロキサシン、塩酸ロメフロキサシン、スルベニシンナトリウム、塩酸セフメノキシム、ベンジルペニシリンカリウム、硫酸ベルベリン、塩化ベルベリン、コリスチンメタスルホン酸ナトリウム、エリスロマイシン、ラクトビオン酸エリスロマイシン、キタサマイシン、スピラマイシン、硫酸フラジオマイシン、硫酸ポリミキシン、ジベカシン、アミカシン、硫酸アミカシン、アシクロビル、イオドデオキシサイチジン、イドクスウリジン、シクロサイチジン、シトシンアラビノシド、トリフルオロチミジン、ブロモデオキシウリジン、ポリビニルアルコールヨウ素、ヨウ素、アムホテリシンB、イソコナゾール、エコナゾール、クロトリマゾール、ナイスタチン、ピマリシン、フルオロシトシン、ミコナゾールなど。 Antibacterial or bactericidal component: for example, aminodeoxykanamycin sulfate, kanamycin sulfate, gentamicin sulfate, sisomycin sulfate, streptomycin sulfate, tobramycin, micronomycin sulfate, alkylpolyaminoethylglycine, chloramphenicol, sulfamethoxazole, Sulfisoxazole, sulfamethoxazole sodium, sulfisoxazole diethanolamine, sulfisoxazole monoethanolamine, sulfisomethazole sodium, sulfisomidine sodium, tetracycline hydrochloride, oxytetracycline hydrochloride, ofloxacin, Norfloxacin, Levofloxacin, Lomefloxacin hydrochloride, Sulbenicin sodium, Cefmenoxime hydrochloride, Benzylpenicillin potassium, Bell sulfate Phosphorus, berberine chloride, colistin sodium metasulfonate, erythromycin, erythromycin lactobionate, kitasamycin, spiramycin, fradiomycin sulfate, polymyxin sulfate, dibekacin, amikacin, amikacin sulfate, acyclovir, iododeoxycytidine, idoxuridine, cyclocydine Tidine, cytosine arabinoside, trifluorothymidine, bromodeoxyuridine, polyvinyl alcohol iodine, iodine, amphotericin B, isoconazole, econazole, clotrimazole, nystatin, pimaricin, fluorocytosine, miconazole.
局所麻酔薬成分:例えば、塩酸オキシブプロカイン、塩酸コカイン、塩酸コルネカイン、塩酸ジブカイン、塩酸テトラカイン、塩酸パラブチルアミノ安息香酸ジエチルアミノエチル、塩酸ピペロカイン、塩酸プロカイン、塩酸プロパラカイン、塩酸ヘキソチオカイン、塩酸リドカインなど。 Local anesthetic components: for example, oxybuprocaine hydrochloride, cocaine hydrochloride, cornecaine hydrochloride, dibucaine hydrochloride, tetracaine hydrochloride, diethylaminoethyl parabutylaminobenzoate, piperocaine hydrochloride, procaine hydrochloride, proparacaine hydrochloride, hexothiocaine hydrochloride, lidocaine hydrochloride.
ステロイド成分:例えば、デキサメタゾン、ヒドロコルチゾン、フルオロメトロン、プレドニゾロン、メチルプレドニゾロン、ヒドロキシメステロン(hydroxymesterone)、カプロン酸ヒドロコルチゾン、カプロン酸プレドニゾロン、酢酸コルチゾン、酢酸ヒドロコルチゾン、酢酸プレドニゾロン、デキサメタゾンメタスルホベンゾエートナトリウム、デキサメタゾン硫酸ナトリウム、デキサメタゾンリン酸ナトリウム、トリアムシノロンアセトニド、ベタメタゾンリン酸ナトリウム、メタスルホ安息香酸デキサメタゾンナトリウム、メチルプレドニゾロンなど。 Steroid component: for example, dexamethasone, hydrocortisone, fluorometholone, prednisolone, methylprednisolone, hydroxymesterone, hydrocortisone caproate, prednisolone caproate, cortisone acetate, hydrocortisone acetate, prednisolone acetate, sodium dexamethasone metasulfobenzoate, sodium dexamethasone sulfate Dexamethasone sodium phosphate, triamcinolone acetonide, betamethasone sodium phosphate, dexamethasone sodium metasulfobenzoate, methylprednisolone and the like.
緑内障治療成分:例えば、イソプロピルウノプロストン、エピネフリン、塩酸アプラクロニジン、塩酸カルテオロール、塩酸ジピベフリン、塩酸ドルゾラミド、塩酸ピロカルピン、塩酸ブナゾシン、塩酸ブプラノロール、塩酸ベタキソロール、塩酸ベフノロール、カルバコール、塩酸レボブノロール、ジピバル酸エピネフリン、臭化ジスチグミン、ニプラジロール、マレイン酸チモロール、ラタノプロストなど。 Glaucoma treatment components: for example, isopropyl unoprostone, epinephrine, apraclonidine hydrochloride, carteolol hydrochloride, dipivefrin hydrochloride, dorzolamide hydrochloride, pilocarpine hydrochloride, bunazosin hydrochloride, bupranolol hydrochloride, betaxolol hydrochloride, befnolol hydrochloride, carbachol, levobunolol hydrochloride, epinephrine hydrochloride , Distigmine bromide, nipradilol, timolol maleate, latanoprost and the like.
白内障治療成分:例えば、グルタチオン、ピレノキシン、5,12−ジヒドロアザペンタセンジスルホン酸ナトリウム(Sodium 5,12-dihydro azapentacene disulfonate)など。 Cataract treatment component: for example, glutathione, pirenoxine, sodium 5,12-dihydroazapentacene disulfonate and the like.
解熱鎮痛薬成分:例えば、アセチルサリチル酸、アセトアミノフェン、ラクチルフェネチジンなど。
鎮静催眠薬成分:例えば、ブロムワレリル尿素、アリルイソプロピルアセチル尿素など。
鎮咳薬成分:アクロラミド、クロペラスチン、ペントキシベリン(カルベタペンタン)、チペピジン、ジブナート、デキストロメトルファン、コデイン、ジヒドロコデイン、ノスカピンおよびそれらの薬理学的に許容される塩(例えば、塩酸クロペラスチン、ヒベンズ酸チペピジン、臭化水素酸デキストロメトルファン、リン酸コデイン、リン酸ジヒドロコデイン、塩酸ノスカピンなど)など。
Antipyretic analgesic component: for example, acetylsalicylic acid, acetaminophen, lactylphenetidine and the like.
Sedative hypnotic ingredients: for example, bromvalerylurea, allylisopropylacetylurea, etc.
Antitussive ingredients: achloramide, cloperastine, pentoxyberine (carbetapentane), tipepidine, dibutate, dextromethorphan, codeine, dihydrocodeine, noscapine and their pharmacologically acceptable salts (eg cloperastine hydrochloride, tipepidine hibenzate) Dextromethorphan hydrobromide, codeine phosphate, dihydrocodeine phosphate, noscapine hydrochloride, etc.).
気管支拡張薬成分または交感神経興奮薬成分:エフェドリン、メチルエフェドリン、シュードエフェドリン、トリメトキノール、メトキシフェナミンおよびそれらの薬理学的に許容される塩(例えば、塩酸エフェドリン、塩酸メチルエフェドリン、塩酸シュードエフェドリン、塩酸トリメトキノール、塩酸メトキシフェナミンなど)など。
去痰薬成分:グアヤコールスルホン酸ナトリウム、グアイフェネシンなど。
生薬成分:カンゾウ、キキョウ、ウイキョウ、カミツレ、ケイヒ、葛根湯など。
Bronchodilator component or sympathomimetic component: ephedrine, methylephedrine, pseudoephedrine, trimethquinol, methoxyphenamine and pharmacologically acceptable salts thereof (for example, ephedrine hydrochloride, methylephedrine hydrochloride, pseudoephedrine hydrochloride) , Trimethquinol hydrochloride, methoxyphenamine hydrochloride, etc.).
Expectorant ingredient: sodium guaiacol sulfonate, guaifenesin, etc.
Herbal medicine ingredients: licorice, kikyo, fennel, chamomile, keihi, kakkonto, etc.
本発明の組成物に対して、これらの成分の配合量は、製剤の種類、活性成分の種類などに応じて適宜選択され、眼科用製剤、内服用製剤などにおける各種成分の配合量は当該技術分野で既知である。例えば、水性組成物の場合、製剤全体に対して0.0001〜30w/v%、好ましくは、0.001〜10w/v%程度の範囲から選択できる。また、内服用製剤の場合、成人一日服用量0.01〜10000mg、好ましくは0.1〜1000mg程度の範囲から選択できる。 For the composition of the present invention, the blending amounts of these components are appropriately selected according to the type of formulation, the type of active ingredient, etc., and the blending amounts of various components in ophthalmic preparations, internal preparations, etc. Known in the field. For example, in the case of an aqueous composition, it can be selected from the range of about 0.0001 to 30 w / v%, preferably about 0.001 to 10 w / v% with respect to the whole preparation. In the case of a preparation for internal use, the daily dose for adults can be selected from a range of 0.01 to 10000 mg, preferably about 0.1 to 1000 mg.
また、本発明の組成物には、発明の効果を損なわない範囲であれば、その用途や形態に応じて、医薬品、医薬部外品などに使用される様々な成分や添加物を適宜選択し、併用して製剤化することが可能である。例えば、液剤などの調製に一般的に使用される担体(水、水性溶媒、水性または油性基剤など)、ガム質、多糖類などの高分子化合物、糖類、糖アルコール類、界面活性剤、等張化剤、香料または清涼化剤、安定剤、溶解剤、基剤など、固形剤では、結合剤、賦形剤、滑沢剤、崩壊剤、発泡剤などの各種添加剤を挙げることができる。本発明において好適な成分としては、例えば、次のような成分が挙げられる。 In addition, in the composition of the present invention, various components and additives used for pharmaceuticals, quasi drugs and the like are appropriately selected depending on the use and form as long as the effects of the invention are not impaired. It is possible to formulate it in combination. For example, carriers (water, aqueous solvents, aqueous or oily bases, etc.) commonly used in the preparation of liquids, gums, polymer compounds such as polysaccharides, saccharides, sugar alcohols, surfactants, etc. Solid agents such as tonicity agents, fragrances or refreshing agents, stabilizers, solubilizers, bases, and the like can include various additives such as binders, excipients, lubricants, disintegrants, and foaming agents. . Examples of suitable components in the present invention include the following components.
ガム質、多糖類などの高分子化合物:例えば、カラヤガム、キサンタンガム、キャロブガム、グアーガム、グアヤク脂、クインスシード、トラガント、ベンゾインゴム、ローカストビーンガム、カゼイン、寒天、アルギン酸、デキストリン、シクロデキストリン、デキストラン、ガラギーナン、ゼラチン、コラーゲン、ペクチン、デンプン、ポリガラクツロン酸、キチンおよびその誘導体、キトサンおよびその誘導体、エラスチン、ヘパリン、ヘパリノイド、ヘパリン硫酸、ヘパラン硫酸、ヒアルロン酸、セラミド、ポリビニルメタアクリレート、ポリアクリル酸、ポリエチレンイミン、リボ核酸、デオキシリボ核酸など、およびその薬学上許容される塩類など。 High molecular compounds such as gums and polysaccharides: for example, Karaya gum, xanthan gum, carob gum, guar gum, guaiac gum, quince seed, tragacanth, benzoin gum, locust bean gum, casein, agar, alginic acid, dextrin, cyclodextrin, dextran, garaginan , Gelatin, collagen, pectin, starch, polygalacturonic acid, chitin and its derivatives, chitosan and its derivatives, elastin, heparin, heparinoid, heparin sulfate, heparan sulfate, hyaluronic acid, ceramide, polyvinyl methacrylate, polyacrylic acid, polyethyleneimine Ribonucleic acid, deoxyribonucleic acid and the like, and pharmaceutically acceptable salts thereof.
糖類:例えばフルクトース、ガラクトース、マンノース、リボース、アロース、リブロース、アラビノース、キシロース、リキソース、デオキシリボース、マルトース、トレハロース、スクロース、セロビオース、グルコビオース、ビシアノース、ルチノース、ラクトース、プルラン、ラクツロース、ラフィノース、マルチトール、スタキオースなど。
糖アルコール類:例えば、キシリトール、マンニトールなど。
Sugars: for example fructose, galactose, mannose, ribose, allose, ribulose, arabinose, xylose, lyxose, deoxyribose, maltose, trehalose, sucrose, cellobiose, glucobiose, vicyanose, lutinose, lactose, pullulan, lactulose, raffinose, maltitol, stachyose Such.
Sugar alcohols: For example, xylitol, mannitol and the like.
界面活性剤:例えば、アルキルジアミノエチルグリシンなどのグリシン型両性界面活性剤;アルキル4級アンモニウム塩(具体的には、塩化ベンザルコニウム、塩化ベンゼトニウムなどの陽イオン界面活性剤など。 Surfactant: For example, glycine-type amphoteric surfactant such as alkyldiaminoethylglycine; alkyl quaternary ammonium salt (specifically, cationic surfactant such as benzalkonium chloride and benzethonium chloride).
等張化剤:例えば、亜硫酸水素ナトリウム、亜硫酸ナトリウム、塩化カリウム、塩化カルシウム、塩化ナトリウム、塩化マグネシウム、酢酸カリウム、酢酸ナトリウム、炭酸水素ナトリウム、炭酸ナトリウム、チオ硫酸ナトリウム、硫酸マグネシウム、リン酸水素二ナトリウム、リン酸二水素ナトリウム、リン酸二水素カリウム、グリセリン、プロピレングリコールなど。 Isotonizing agents: for example, sodium bisulfite, sodium sulfite, potassium chloride, calcium chloride, sodium chloride, magnesium chloride, potassium acetate, sodium acetate, sodium bicarbonate, sodium carbonate, sodium thiosulfate, magnesium sulfate, dihydrogen phosphate Sodium, sodium dihydrogen phosphate, potassium dihydrogen phosphate, glycerin, propylene glycol and the like.
香料又は清涼化剤:例えば、アネトール、オイゲノール、リュウノウ、ウイキョウ油、大茴香油、丁子油、アニス油、ケイヒ油など。 Perfume or refreshing agent: for example, anethole, eugenol, ryuunou, fennel oil, bonito perfume oil, clove oil, anise oil, cinnamon oil and the like.
安定剤:ジブチルヒドロキシトルエン、トロメタモール、ナトリウムホルムアルデヒドスルホキシレート(ロンガリット)、トコフェロール、ピロ亜硫酸ナトリウム、モノエタノールアミン、モノステアリン酸アルミニウムなど。 Stabilizer: Dibutylhydroxytoluene, trometamol, sodium formaldehyde sulfoxylate (Longalite), tocopherol, sodium pyrosulfite, monoethanolamine, aluminum monostearate, etc.
溶解剤、基剤:オクチルドデカノール、オリーブ油、ゴマ油、酸化チタン、臭化カリウム、ダイズ油、ツバキ油、トウモロコシ油、ナタネ油、パラフィン、ヒマシ油、プラスチベース、ラッカセイ油、ラノリン、ワセリンなど。 Solubilizer, base: octyldodecanol, olive oil, sesame oil, titanium oxide, potassium bromide, soybean oil, camellia oil, corn oil, rapeseed oil, paraffin, castor oil, plastibase, peanut oil, lanolin, petrolatum and the like.
賦形剤:ショ糖、乳糖、デンプン、コーンスターチ、結晶セルロース、軽質無水ケイ酸など。
滑沢剤:ステアリン酸マグネシウムなど。
崩壊剤:クロスカルメロースナトリウムなど。
発泡剤:炭酸水素ナトリウムなど。
Excipients: Sucrose, lactose, starch, corn starch, crystalline cellulose, light anhydrous silicic acid, etc.
Lubricant: Magnesium stearate, etc.
Disintegrant: croscarmellose sodium and the like.
Foaming agent: sodium bicarbonate and the like.
本発明の組成物は、公知の方法により製造できる。例えば、点眼剤または洗眼剤では、蒸留水又は精製水及び添加剤を用いてプラノプロフェン又はその塩およびビタミンB2類とを溶解させ、所定の浸透圧及びpHに調整し、無菌環境下、ろ過滅菌処理し、洗浄滅菌済みの容器に無菌充填することにより製造できる。 The composition of this invention can be manufactured by a well-known method. For example, in an eye drop or eye wash, pranoprofen or a salt thereof and vitamin B 2 are dissolved using distilled water or purified water and additives, adjusted to a predetermined osmotic pressure and pH, It can be manufactured by sterilizing by filtration and aseptically filling containers that have been sterilized by washing.
以下、実施例及び比較例を示し、本発明を具体的に説明するが、本発明は下記の実施例に制限されるものではない。 EXAMPLES Hereinafter, although an Example and a comparative example are shown and this invention is demonstrated concretely, this invention is not restrict | limited to the following Example.
試験例1 疲労度自己評価試験
表1に記載の処方に従い、各成分を精製水に溶解して全量を100mLとして試験液を調製した。
健常人4名に対して、VDT作業前、VDT作業開始1時間後、2時間後に比較例1の試験液を両眼に点眼し、2時間後の点眼の後、疲労度の自己評価を行った。評価基準および評価項目は、中村芳子、「眼精疲労の診断と対策」、新しい眼科、第14巻、第9号、p.1319−1326に従い、下記5段階の評価基準で18個の評価項目について被験者に点数をつけてもらい、点数の合計を疲れ目度とした。同様に比較例2、3および実施例1の試験液についても疲れ目度を評価した。
各試験液について評価した疲れ目度から、下記式に従って、比較例1点眼後を基準にして自己評価改善値を算出した。
自己評価改善値=疲れ目度(比較例1点眼後)−疲れ目度(試験液点眼後)
<評価基準>
0:いいえ
1:症状はあるが、気にするほどではない
2:症状があり気になるが、そのままにしている
3:そのままにしておけないので、誰かに相談しようと思う
4:治療を必要とするほど症状が強く、仕事に差し支える
<評価項目>
目が疲れる、目の奥が痛い、目がかすむ、涙が出る、充血する、目が熱い感じがする、目がだるい・重い・圧迫感がある、目が乾く、まぶしい、目を開けているのがつらい、ぼやけて見える、二重に見える、目に異物感がある、距離が変わるとすぐ焦点が合わない、頭痛がする、めまい・立ちくらみがする、肩こり・腰痛がある、頭が重い
結果を表1に示す。
Test example 1 Fatigue self-assessment test
According to the formulation described in Table 1, each component was dissolved in purified water to prepare a test solution with a total volume of 100 mL.
For 4 healthy subjects, the test solution of Comparative Example 1 was instilled into both eyes before VDT work, 1 hour after the start of VDT work, and 2 hours later, and after 2 hours of instillation, self-assessment of fatigue was performed. It was. The evaluation criteria and evaluation items are 18 evaluation items according to the following five-step evaluation criteria according to Yoshiko Nakamura, “Diagnosis and Countermeasures for Eye Fatigue”, New Ophthalmology, Vol. 14, No. 9, pages 1319–1326. The subject was given a score for and the total score was taken as the fatigue level. Similarly, the fatigue strength of the test solutions of Comparative Examples 2 and 3 and Example 1 was also evaluated.
From the degree of fatigue evaluated for each test solution, a self-evaluation improvement value was calculated according to the following formula on the basis of one eye point after Comparative Example.
Self-assessment improvement value = Fatigue degree (after 1 eye of Comparative Example) −Fatigue degree (after eye drop of test solution)
<Evaluation criteria>
0: No 1: Symptom is not enough to worry 2: Symptom is worrisome, but is left as it is 3: Cannot be left as it is, so I would like to consult someone 4: Need treatment <Assessment>
Eyes are tired, back of eyes hurts, eyes are blurred, tears are born, blood is congested, eyes are hot, eyes are dull / heavy / compressed, eyes are dry, dazzling, eyes are open Painful, blurry, double-looking, foreign body sensation, out of focus as distance changes, headache, dizziness / dizziness, stiff shoulders / backache, heavy head The results are shown in Table 1.
比較例2、3から、プラノプロフェンまたはフラビンアデニンジヌクレオチドナトリウムにも、それぞれ疲れ目度の自己評価を若干改善する効果があることがわかるが、プラノプロフェンおよびフラビンアデニンジヌクレオチドナトリウムをともに含有する実施例1では、疲れ目度の自己評価が顕著に改善することが確認された。 From Comparative Examples 2 and 3, it can be seen that pranoprofen or flavin adenine dinucleotide sodium also has an effect of slightly improving the self-evaluation of the fatigue degree, but both pranoprofen and flavin adenine dinucleotide sodium are contained. In Example 1, it was confirmed that the self-evaluation of the fatigue degree significantly improved.
試験例2 ピント調節速度測定試験
試験例1の評価終了後、直ちにピント調節力測定器(アコモドメーター AR3−SV6:ニデック社製)を用いて、被験者4名のピント調節力範囲内(4〜5D)に設定された遠指標と近指標を5秒間の交互呈示として凝視させ(ステップ方法)、遠指標から近指標に移ったときの毛様体筋の緊張速度(GRAD値(cm/sec))を3回測定し、その平均値を求めた。緊張速度が大きい(GRAD値の絶対値が大きい)とピント調節速度が速いことを示す。測定した各試験サンプルのGRAD値から、下記式に従って、比較例1点眼後を基準にして調節速度改善率(%)を算出した。
調節速度改善率(%)=GRAD値(試験液点眼後の平均値)/GRAD値(比較例1点眼後の平均値)×100
結果を表2に示す。
Test example 2 Focus adjustment speed measurement test
Immediately after the evaluation of Test Example 1 was completed, the far index set within the focus adjustment force range (4 to 5D) of the four subjects using the focus adjustment force measuring instrument (Accomodometer AR3-SV6: manufactured by Nidec Co.). And the near index are stared as alternate presentations for 5 seconds (step method), and the tension velocity (GRAD value (cm / sec)) of the ciliary muscle when moving from the far index to the near index is measured three times. The average value was obtained. Large tension speed (large absolute value of GRAD value) indicates fast focus adjustment speed. From the measured GRAD value of each test sample, the adjustment speed improvement rate (%) was calculated according to the following formula, based on the eyedrop after the first eyedrop of Comparative Example.
Adjustment rate improvement rate (%) = GRAD value (average value after instillation of test solution) / GRAD value (average value after instillation of 1 comparative example) × 100
The results are shown in Table 2.
比較例2、3から、プラノプロフェンまたはフラビンアデニンジヌクレオチドナトリウムにも、それぞれピント調節速度を上げる効果があることがわかるが、プラノプロフェンおよびフラビンアデニンジヌクレオチドナトリウムをともに含有する実施例1では、ピント調節速度が顕著に向上することが確認された。 From Comparative Examples 2 and 3, it can be seen that pranoprofen or flavin adenine dinucleotide sodium also has an effect of increasing the focus control rate, but in Example 1 containing both pranoprofen and flavin adenine dinucleotide sodium, It was confirmed that the focus adjustment speed was significantly improved.
以下に製剤実施例を挙げる。
以下の実施例中の配合量は、適量または特に単位の記載のないものについてはすべてw/v%を表す。また、実施例2〜19は、ポリエチレンナフタレート10%とポリエチレンテレフタレート90%の混合体の容器(340nm〜380nmの吸光度3.0以上)に充填し、25℃の下、0.5万lxの光を6時間連続照射し、積算照射量3万lx・hrの光に曝光したところ、実施例2〜19すべてにおいてプラノプロフェンの残存率が90%以上に維持された。
The formulation examples are given below.
The compounding amounts in the following examples all represent w / v% in the case of an appropriate amount or a unit not particularly described. In Examples 2 to 19, a container of a mixture of 10% polyethylene naphthalate and 90% polyethylene terephthalate (absorbance of 340 nm to 380 nm of 3.0 or more) was filled, and light at 50,000 lx was applied at 25 ° C. for 6 hours. When continuously irradiated and exposed to light with an integrated irradiation amount of 30,000 lx · hr, in all of Examples 2 to 19, the residual ratio of pranoprofen was maintained at 90% or more.
実施例20 錠剤:1錠中
プラノプロフェン 75mg
フラビンアデニンジヌクレオチドナトリウム 2mg
ヒドロキシプロピルセルロース 17mg
ステアリン酸マグネシウム 2mg
結晶セルロース 適量
合 計 180mg
日本薬局方製剤総則、「錠剤」の製造方法に準じて1錠あたり180mgの錠剤(1日3回、1回あたり1錠を服用する錠剤)を製造した。より具体的には、ステアリン酸マグネシウム以外の成分を混合し造粒する。その後、ステアリン酸マグネシウムを均一になるまで混合した後、打錠して錠剤を製した。
Example 20 Tablet: 1 tablet of pranoprofen 75 mg
Flavin adenine dinucleotide sodium 2mg
Hydroxypropylcellulose 17mg
Magnesium stearate 2mg
Crystalline cellulose
180mg total
According to the Japanese Pharmacopoeia General Rules for Preparation, “Tablets”, 180 mg tablets (tablets taken 1 tablet 3 times a day) were manufactured. More specifically, ingredients other than magnesium stearate are mixed and granulated. Thereafter, magnesium stearate was mixed until uniform, and then tableted to produce tablets.
実施例21 錠剤:1錠中
プラノプロフェン 35mg
リン酸リボフラビンナトリウム 2mg
ヒドロキシプロピルセルロース 17mg
ステアリン酸マグネシウム 2mg
結晶セルロース 適量
合 計 180mg
日本薬局方製剤総則、「錠剤」の製造方法に準じて1錠あたり180mgの錠剤(1日3回、1回あたり1錠を服用する錠剤)を製造した。より具体的には、ステアリン酸マグネシウム以外の成分を混合し造粒する。その後、ステアリン酸マグネシウムを均一になるまで混合した後、打錠して錠剤を製した。
Example 21 Tablet: 1 tablet of pranoprofen 35 mg
Riboflavin sodium phosphate 2mg
Hydroxypropylcellulose 17mg
Magnesium stearate 2mg
Crystalline cellulose
180mg total
According to the Japanese Pharmacopoeia General Rules for Preparation, “Tablets”, 180 mg tablets (tablets taken 1 tablet 3 times a day) were manufactured. More specifically, ingredients other than magnesium stearate are mixed and granulated. Thereafter, magnesium stearate was mixed until uniform, and then tableted to produce tablets.
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